RS370666667 FGFR1

Health Risk Chr 8:38429954
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Associated Conditions
Inborn genetic diseases
Pfeiffer syndrome
Hypogonadotropic hypogonadism 2 with or without anosmia
Inborn genetic diseases
Pfeiffer syndrome
Hypogonadotropic hypogonadism 2 with or without anosmia
Other Variants in FGFR1
rs121909627 rs1586111679 rs1563433902 rs121909628 rs121909629 rs1586287678 rs121909630 rs121909632 rs121909631 rs121909633
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